"Center for Pediatric Genomic Medicine, Children's Mercy Hospital and - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 337104	NM_006302.3(MOGS):c.2353G>A (p.Gly785Ser)	MOGS (G785S +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 95358	NM_006302.3(MOGS):c.1838G>A (p.Arg613Gln)	MOGS (R613Q +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 235622	NM_006302.3(MOGS):c.881C>T (p.Pro294Leu)	MOGS (P294L +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign

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